염소화 뇌유
염소화뇌유 · 염소화캄펜 · 톡사펜 · 게니펜 · 스트로바넷 · 스트로반 · 아나톡스 · 알톡스

식별자 및 물리적 특성
| CAS No. | 1852481-29-8 |
|---|---|
| 분자식 | C10H8Cl8 |
| 평균 분자량 | 411.8 g/mol |
| 단동위원소 질량 | 407.813422 g/mol |
| SMILES | C=C1C(CCl)(CCl)C2(Cl)C(Cl)C(Cl)C1(Cl)C2(Cl)Cl |
| InChIKey | OEJNXTAZZBRGDN-UHFFFAOYSA-N |
| PubChem CID | 5284469 |
| ChEMBL | CHEMBL1339089 |
| EC No. | 232-283-3 |
| DTXSID | DTXSID90858936 |
| 현지명 | 염소화 뇌유 |
화학 및 물리적 성질
| XLogP | 4.7 |
|---|---|
| 극성 표면적 | 0 |
| 수소 결합 공여자 수 | 0 |
| 수소 결합 수용자 수 | 0 |
| 회전 가능 결합 수 | 2 |
| 무거운 원자 수 | 18 |
| 형식 전하 | 0 |
| 복잡도 | 403 |
| 물질 분류 | Hazardous Air Pollutants (HAPs)Carcinogens |
| 화장품 | Cosmetics ingredient -> Fragrance |
| 농약 | Pesticide -> EPA IRISAgrochemicals -> Pesticide active substancesActive substance -> EU Pesticides database: Not approvedPesticides -> Organochlorine PesticidesPesticide (Toxaphene) -> USDA PDB |
| LogP(분배 계수) | The median log Kow for toxaphene is 5.90.3.35.5 |
| 냄새 | Pleasant piney odorMild odor of chlorine and camphorMild, turpentine-like odorMild, piney, chlorine- and camphor-like odor. |
| 밀도 | 1.65 (EPA, 1998) - Denser than waterwill sink1.65 @ 25 °CRelative density (water = 1): 1.651.65 @25 °C |
| Color/Form | Yellow waxy solid.Amber, waxy solid. |
| 용해도 | less than 1 mg/mL at 66 °F (NTP, 1992)Clear, amber-colored, and viscous liquid, mild terpene odor, specific gravity: 1.519-1.567 at 25 °C/25 °Creadily sol in most commercial organic solvents and is more sol in aromatic than in aliphatic hydrocarbons /Strobane T-90/Freely sol in aromatic hydrocarbonsREADILY SOL IN ORG SOLVENTS INCL PETROLEUM OILS3 mg/l water @ room temp> 450 g/100 ml benzene25~30°C에서 알코올 120g/L(인용, Meites, 1963) |
| Corrosivity | Noncorrosive in the absence of moistureCorrosive to ironSolution in xylene may produce corrosive products when heated. |
| 인화점 | 84 °F (EPA, 1998)135 °C, 275 °F (closed cup) /Chlorinated camphene 60%/115 °C (tag closed cup) /Toxaphene 90% soln/34-46 °C (tag closed cup) /Strobane T-90/4 °C |
| 끓는 점 | Decomposes (NTP, 1992)Decomposes near boiling point |
| 녹는점 | 149 to 194 °F (EPA, 1998)65-90 °C149-194 °F65-90℃ |
| 증기압 | 15.8 at 25 °C (2,2,5-endo-6-exo-8,9,10-heptachlorobornane, toxaphene component, Hinckley etal., 1990) |
| 저장 조건 | 2-8°C |
| 물리적 상태 | 노란색 왁스 같은 고체 |
| 용해도 | 0.4mg/L(25℃) |
| Merck | 13,9633 |
| 헨리 상수 | 0.99 at 10 °C, 3.56 at 20 °C, 6.81 at 30 °C, 8.49 at 35 °C, 14.8 at 40 °C (gas stripping, Jantunen and Bidleman, 2000) |
| 안정성 | 안정적인. 알칼리, 강산화제와 호환되지 않습니다. 열과 빛에 민감합니다. |
| EPA | Toxaphene (8001-35-2) |
화학적 성질
yellow waxy solid
안전 및 규제
| GHS 분류 | DangerH301: Toxic if swallowed [Danger Acute toxicity, oral]P203, P261, P264, P270, P271, P273, P280, P301+P316, P302+P352, P304+P340, P317, P318, P319, P321, P330, P332+P317, P362+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)H301 (97.6%): Toxic if swallowed [Danger Acute toxicity, oral] |
|---|---|
| 규제 정보 | Hazard Traits - BioaccumulationCarcinogenicityEnvironmental PersistenceNeurotoxicityRespiratory ToxicityRegulation (EC) No 178/2002 (amended)Substance: ToxapheneThe New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.) |
| 기타 안전 정보 | IMAP assessments - Toxaphene: Human health tier I assessment |
| 운송 라벨(DOT) | Poison |
| 화재 위험 | Container may explode in heat of fire. Toxic vapors are generated when heated. Releases hydrochloric acid in the presence of alkali, on prolonged exposure to sunlight, and at temperatures above 311F. Avoid strong oxidizers, corrosive to iron. (EPA, 1998)Liquid formulations containing organic solvents may be flammable. Gives off irritating or toxic fumes (or gases) in a fire. |
| 화재 가능성 | Solid /is/ not flammable, but /it is/ usually dissolved in combustible liquid. |
| 건강 유해성 | Camphechlor is extremely toxic: the probable oral lethal dose (human) is 5-50 mg/kg or between 7 drops and 1 teaspoonful for 70 kg (150 lb.) person. (EPA, 1998) |
| 유해성 요약 | Toxaphene was one of the most heavily used pesticides in the United States in the 1970s and early 1980s. It was used primarily to control insect pests on cotton and other crops in the southern United States. Other uses included controlling insect pests on livestock and killing unwanted fish in lakes. Toxaphene was banned for all registered uses by 1990. Toxaphene is made by reacting chlorine gas with a substance called camphene. The resulting product (toxaphene) is a mixture of hundreds of different chlorinated camphenes and related chemicals.Toxaphene was a widely used pesticide on cotton, other crops, and in livestock and poultry. In 1982, most of its uses were cancelled and in 1990, all uses were cancelled in the United States. The major effect of toxaphene is central nervous system (CNS) stimulation, which results in convulsive seizures. No studies are available on acute (short-term) inhalation exposure to toxaphene in humans or animals. Chronic (long- term) inhalation exposure to toxaphene in humans results in reversible respiratory toxicity, while chronic, oral exposure in animals has resulted in effects on the liver, kidney, spleen, adrenal and thyroid glands, CNS, and the immune system. Animal studies have reported an increased incidence of thyroid gland tumors and liver tumors via ingestion. EPA has classified toxaphene as a Group B2, probable human carcinogen. |
용도
용도
Toxaphene is an insecticide that contains over 200–700 chemicals and can exist as an yellow to amber solid or gas. Heavily used in the United States until 1982, its use was completely banned in 1990. Toxaphene was used primarily to control insects on cotton crops in the southern United States; it has also been used to control pests on livestock and to control unwanted fish in aquatic environments. Reports have indicated that fish are low metabolizers of toxaphene, whereas other aquatic life such as snails can be extensive metabolizers, thus reducing the toxicity of toxaphene to aquatic life other than fish (Isensee et al., 1979).
일반 설명
Yellow, waxy solid with a pleasant piney odor. Used as an insecticide, primarily for cotton and early growth stages of vegetables. Also peas, soybeans, peanut, corn, and wheat. Not produced commercially in the U.S. since 1982. Only registered for scabies control on cattle in the U.S.